# Mahe-Medizintechnik

- Location (FDA's records): Nashville, TN
- FDA decisions: 8 (1993–1994): 8 510(k) clearances
- Product codes: GCJ (3), LXH (1), HFB (1), LRC (1), GEI (1), HET (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K942821: Mahe Instruments (Nov 2, 1994)
- K942819: Trocar with Shield (Aug 23, 1994)
- K933768: Coagulator, Laparoscopic, Lunipolar/Accessories (Jun 27, 1994)
- K933767: Forceps, Biopsy Gynecological Instru/Biopsy (May 26, 1994)
- K933770: Forceps, Ent Instr, Ent Manual Surg Retract/All Type (Mar 23, 1994)
- K935442: Mahe Instruments (Mar 14, 1994)
- K933772: Punch Surgical (Feb 1, 1994)
- K925624: Microsurgical Instruments (Jul 22, 1993)

Source page: https://510kreport.com/company/mahe-medizintechnik